Specific Roles of Kal-1 in Olfaction: A Model of Kallmann Syndrome in Drosophila

The X chromosome-linked form of Kallmann syndrome (KS) is caused by disruption of the Kal-1 gene, which encodes a secreted protein called Anosmin-1. The definitive features of the KS phenotype are anosmia and hypogonadism. Despite high conservation of the Kal-1 gene from invertebrates to vertebrates, the Kal-1 homolog in mice has not been identified. The unavailability of an animal model has hampered research on the disease in vivo. Hence, little is known about the cellular processes and molecular functions underlying KS. Here, I isolated a Drosophila kal-1 null mutant, which removes the entire kal-1 coding region. Antibody staining shows that Anosmin-1 specifically localizes to the dendrites of olfactory receptor neurons (ORNs) throughout development. The dendrites of ORNs sense odorants in the environment including the Drosophila melanogaster male-specific pheromone 11-cis-vaccenyl acetate, which is known to inhibit male-male mating behaviors. Interestingly, mutant males that lack kal-1 function inappropriately court other males. These results imply a possible role of kal-1 in mating behaviors in part by mediating pheromone perception.

Name thesis:degree_name

Ph.D.

Level thesis:degree_level

Dissertation

Discipline thesis:degree_discipline

Neuroscience

Grantor

University of Illinois at Urbana-Champaign

Year dc:date

2015

Author dc:creator

• Ozawa, Rie

Contributors dc:contributor

• Stephanie Ceman

• Biology, Neuroscience

Language dc:language

eng

Identifier

(MiAaPQ)AAI3347493

OAI identifier oai:identifier

oai:www.ideals.illinois.edu:2142/82525